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On page 269 showing 5361 ~ 5380 out of 256,031 results
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  • RRID:CVCL_M941

https://web.expasy.org/cellosaurus/CVCL_M941

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.

Proper citation: Coriell Cat# GM03721, RRID:CVCL_M941 Copy   


  • RRID:CVCL_X296

https://web.expasy.org/cellosaurus/CVCL_X296

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(6)(6qter->6p25::1q32->1qter)mat (Coriell=GM03647)., Population: Caucasian.

Proper citation: Coriell Cat# GM03647, RRID:CVCL_X296 Copy   


  • RRID:CVCL_7397

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7397

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM03652, RRID:CVCL_7397 Copy   


  • RRID:CVCL_X107

https://web.expasy.org/cellosaurus/CVCL_X107

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,del(Y)(pter->q11) [42]; 45,X [8] (Coriell=GM03595)., Population: Caucasian.

Proper citation: RRID:CVCL_X107 Copy   


  • RRID:CVCL_AB33

https://web.expasy.org/cellosaurus/CVCL_AB33

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_AB33 Copy   


  • RRID:CVCL_V471

https://web.expasy.org/cellosaurus/CVCL_V471

Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_V471 Copy   


  • RRID:CVCL_X107

https://web.expasy.org/cellosaurus/CVCL_X107

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,del(Y)(pter->q11) [42]; 45,X [8] (Coriell=GM03595)., Population: Caucasian.

Proper citation: Coriell Cat# GM03595, RRID:CVCL_X107 Copy   


  • RRID:CVCL_DF20

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_DF20

Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Transformed cell line
Comments:

Proper citation: Coriell Cat# GM03640, RRID:CVCL_DF20 Copy   


  • RRID:CVCL_7400

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_7400

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_7400 Copy   


  • RRID:CVCL_X452

https://web.expasy.org/cellosaurus/CVCL_X452

Organism: Homo sapiens (Human)
Disease: Maroteaux-Lamy syndrome
Category: Finite cell line
Comments: Population: African American.

Proper citation: Coriell Cat# GM03722, RRID:CVCL_X452 Copy   


  • RRID:CVCL_F201

https://web.expasy.org/cellosaurus/CVCL_F201

Organism: Homo sapiens (Human)
Disease: Menkes disease
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_F201 Copy   


  • RRID:CVCL_5M86

https://web.expasy.org/cellosaurus/CVCL_5M86

Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Finite cell line
Comments: Population: Caucasian; Iberian.

Proper citation: RRID:CVCL_5M86 Copy   


  • RRID:CVCL_U396

https://web.expasy.org/cellosaurus/CVCL_U396

Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_U396 Copy   


  • RRID:CVCL_AK84

https://web.expasy.org/cellosaurus/CVCL_AK84

Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM03833, RRID:CVCL_AK84 Copy   


  • RRID:CVCL_AK79

https://web.expasy.org/cellosaurus/CVCL_AK79

Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Finite cell line
Comments: Population: Caucasian; German.

Proper citation: Coriell Cat# GM03824, RRID:CVCL_AK79 Copy   


  • RRID:CVCL_1H63

https://web.expasy.org/cellosaurus/CVCL_1H63

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian.

Proper citation: Coriell Cat# GM03748, RRID:CVCL_1H63 Copy   


  • RRID:CVCL_1H64

https://web.expasy.org/cellosaurus/CVCL_1H64

Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments:

Proper citation: RRID:CVCL_1H64 Copy   


  • RRID:CVCL_X111

https://web.expasy.org/cellosaurus/CVCL_X111

Organism: Homo sapiens (Human)
Disease: Deletion 18p syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY,del(18)(qter->p11) (Coriell=GM03767)., Population: Caucasian.

Proper citation: RRID:CVCL_X111 Copy   


  • RRID:CVCL_F193

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_F193

Organism: Homo sapiens (Human)
Disease: Friedreich ataxia
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_F193 Copy   


  • RRID:CVCL_X453

https://web.expasy.org/cellosaurus/CVCL_X453

Organism: Homo sapiens (Human)
Disease: Maroteaux-Lamy syndrome
Category: Transformed cell line
Comments: Population: African American.

Proper citation: Coriell Cat# GM03723, RRID:CVCL_X453 Copy   



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